Hideaki Shiraishi
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Explore the profile of Hideaki Shiraishi including associated specialties, affiliations and a list of published articles.
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Articles
121
Citations
612
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Recent Articles
1.
Imataka G, Shiraishi H
Diseases
. 2025 Jan;
13(1).
PMID: 39851466
Background: Youth suicide remains a significant public health concern in Japan, driven by multifaceted factors such as academic pressures, social isolation, bullying, and family dysfunction. Recent societal changes, including the...
2.
Imataka G, Shiraishi H, Yoshihara S
NeuroSci
. 2025 Jan;
6(1.
PMID: 39846560
Background: Acute disseminated encephalomyelitis (ADEM) is a rare, immune-mediated inflammatory disorder of the central nervous system (CNS), typically characterized by the acute onset of multifocal demyelination. The pathogenesis of ADEM...
3.
Akutsu A, Fujita Y, Hitomi H, Takayanagi F, Ando Y, Imataka G, et al.
Tohoku J Exp Med
. 2025 Jan;
PMID: 39814402
No abstract available.
4.
Imataka G, Mori S, Yui K, Igawa K, Shiraishi H, Yoshihara S
Diseases
. 2024 Dec;
12(12.
PMID: 39727664
Background: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterized by mutations in the TSC1 and TSC2 genes, leading to the dysregulation of the mammalian target of rapamycin...
5.
Takagi Y, Fujita Y, Kano Y, Shiraishi H
J Infect Chemother
. 2024 Dec;
31(3):102599.
PMID: 39725072
The incidence of urinary tract infection (UTI) caused by extensive beta-lactamase-producing Escherichia coli (ESBL-EC) is increasing, including in children. However, the available oral antibiotic treatment options for ESBL-EC are limited....
6.
Fujimoto M, Nakamura Y, Hosoki K, Iwaki T, Sato E, Ieda D, et al.
HGG Adv
. 2024 Aug;
5(4):100342.
PMID: 39169619
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by the loss of function of maternal UBE3A. The major cause of AS is a maternal deletion in 15q11.2-q13, and the...
7.
Noguchi A, Tezuka T, Okuda H, Kobayashi H, Harada K, Yoshida T, et al.
Int J Mol Sci
. 2024 Jul;
25(13).
PMID: 38999942
Familial episodic pain syndrome (FEPS) is an early childhood onset disorder of severe episodic limb pain caused mainly by pathogenic variants of , , and , which encode three voltage-gated...
8.
Anada R, Watanabe H, Shimojo A, Shiraishi H, Yokosawa K
Cereb Cortex
. 2024 Feb;
34(2).
PMID: 38342686
Communication, especially conversation, is essential for human social life. Many previous studies have examined the neuroscientific underpinnings of conversation, i.e. language comprehension and speech production. However, conversation inherently involves two...
9.
Ueda Y, Egawa K, Kawamura K, Ochi N, Goto T, Kimura S, et al.
Brain Dev
. 2023 Dec;
46(3):149-153.
PMID: 38103972
Background: Most long-term affected spinal muscular atrophy (SMA) type 1 patients have severe impairment of motor function and are dependent on mechanical ventilation with tracheostomy. The efficacy and safety of...
10.
Masuda T, Miura S, Sato Y, Tachihara M, Bessho A, Nakamura A, et al.
Sci Rep
. 2023 Nov;
13(1):19729.
PMID: 37957228
Small amounts of epidermal growth factor receptor (EGFR) T790M mutation (micro-T790M), which is detected using droplet digital PCR (ddPCR) but not conventional PCR, in formalin-fixed and paraffin-embedded (FFPE) samples have...